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1
Experimental immunization with anti-rheumatic bacterial extract OM-89 induces T cell responses to heat shock protein (hsp)60 and hsp70; modulation of peripheral immunological tolerance as its possible mode of action in the treatment of rheumatoid arthritis (RA).用抗风湿细菌提取物OM-89进行实验性免疫可诱导T细胞对热休克蛋白(hsp)60和hsp70产生反应;调节外周免疫耐受性作为其治疗类风湿关节炎(RA)的可能作用方式。
Clin Exp Immunol. 1997 Oct;110(1):72-8. doi: 10.1046/j.1365-2249.1997.4841378.x.
2
Antirheumatic E. coli extract OM-89 induces T cell responses to HSP60 and 70.抗风湿性大肠杆菌提取物OM-89诱导T细胞对热休克蛋白60和70产生反应。
Int J Immunopharmacol. 1997 Sep-Oct;19(9-10):565-8. doi: 10.1016/s0192-0561(97)00084-2.
3
Oral administration of HSP-containing E. coli extract OM-89 has suppressive effects in autoimmunity. Regulation of autoimmune processes by modulating peripheral immunity towards hsp's?口服含热休克蛋白的大肠杆菌提取物OM-89对自身免疫具有抑制作用。通过调节外周对热休克蛋白的免疫来调控自身免疫过程?
Biotherapy. 1998;10(3):223-7. doi: 10.1007/BF02678300.
4
Inhibition of adjuvant-induced arthritis by DNA vaccination with the 70-kd or the 90-kd human heat-shock protein: immune cross-regulation with the 60-kd heat-shock protein.用70kd或90kd人热休克蛋白进行DNA疫苗接种对佐剂诱导性关节炎的抑制作用:与60kd热休克蛋白的免疫交叉调节
Arthritis Rheum. 2004 Nov;50(11):3712-20. doi: 10.1002/art.20635.
5
Oral dosing of rats with OM-89 results in the appearance of specific OM-89 antibodies of the IgG2a isotype: possible significance in the treatment of rheumatoid arthritis.给大鼠口服OM-89会导致出现IgG2a亚型的特异性OM-89抗体:这在类风湿性关节炎治疗中的潜在意义。
Int J Immunopharmacol. 1997 Sep-Oct;19(9-10):569-72. doi: 10.1016/s0192-0561(97)00053-2.
6
T cell reactivity to an epitope of the mycobacterial 65-kDa heat-shock protein (hsp 65) corresponds with arthritis susceptibility in rats and is regulated by hsp 65-specific cellular responses.T细胞对分枝杆菌65-kDa热休克蛋白(hsp 65)表位的反应性与大鼠关节炎易感性相关,并受hsp 65特异性细胞反应调控。
Eur J Immunol. 1991 May;21(5):1289-96. doi: 10.1002/eji.1830210529.
7
Heat-shock protein T-cell epitopes trigger a spreading regulatory control in a diversified arthritogenic T-cell response.热休克蛋白T细胞表位在多样化的致关节炎性T细胞应答中触发一种扩展性调节控制。
Immunol Rev. 1998 Aug;164:169-74. doi: 10.1111/j.1600-065x.1998.tb01218.x.
8
Activation of T cells recognizing self 60-kD heat shock protein can protect against experimental arthritis.识别自身60-kD热休克蛋白的T细胞激活可预防实验性关节炎。
J Exp Med. 1995 Mar 1;181(3):943-52. doi: 10.1084/jem.181.3.943.
9
Suppression of adjuvant arthritis in rats by induction of oral tolerance to mycobacterial 65-kDa heat shock protein.
Eur J Immunol. 1996 Nov;26(11):2650-6. doi: 10.1002/eji.1830261116.
10
A conserved mycobacterial heat shock protein (hsp) 70 sequence prevents adjuvant arthritis upon nasal administration and induces IL-10-producing T cells that cross-react with the mammalian self-hsp70 homologue.一种保守的分枝杆菌热休克蛋白(hsp)70序列经鼻腔给药可预防佐剂性关节炎,并诱导产生与哺乳动物自身hsp70同源物发生交叉反应的分泌白细胞介素-10的T细胞。
J Immunol. 2000 Mar 1;164(5):2711-7. doi: 10.4049/jimmunol.164.5.2711.

引用本文的文献

1
Heat shock proteins (HSPs) in the homeostasis of regulatory T cells (Tregs).热休克蛋白在调节性T细胞(Tregs)稳态中的作用
Cent Eur J Immunol. 2016;41(3):317-323. doi: 10.5114/ceji.2016.63133. Epub 2016 Oct 25.
2
Treating arthritis by immunomodulation: is there a role for regulatory T cells?通过免疫调节治疗关节炎:调节性 T 细胞是否有作用?
Rheumatology (Oxford). 2010 Sep;49(9):1632-44. doi: 10.1093/rheumatology/keq130. Epub 2010 May 12.
3
The involvement of heat-shock proteins in the pathogenesis of autoimmune arthritis: a critical appraisal.热休克蛋白在自身免疫性关节炎发病机制中的作用:批判性评价。
Semin Arthritis Rheum. 2010 Oct;40(2):164-75. doi: 10.1016/j.semarthrit.2009.10.002. Epub 2009 Dec 6.
4
Treatment of experimental adjuvant arthritis with the combination of methotrexate and lyophilized Enterococcus faecium enriched with organic selenium.甲氨蝶呤与富含有机硒的冻干屎肠球菌联合治疗实验性佐剂性关节炎
Folia Microbiol (Praha). 2002;47(5):573-8. doi: 10.1007/BF02818800.
5
Arthritis protective regulatory potential of self-heat shock protein cross-reactive T cells.自身热休克蛋白交叉反应性T细胞的关节炎保护调节潜能
Cell Stress Chaperones. 2000 Nov;5(5):452-7. doi: 10.1379/1466-1268(2000)005<0452:aprpos>2.0.co;2.
6
Immunity to heat shock proteins and arthritic disorders.对热休克蛋白的免疫与关节炎疾病
Infect Dis Obstet Gynecol. 1999;7(1-2):49-54. doi: 10.1155/S1064744999000101.

用抗风湿细菌提取物OM-89进行实验性免疫可诱导T细胞对热休克蛋白(hsp)60和hsp70产生反应;调节外周免疫耐受性作为其治疗类风湿关节炎(RA)的可能作用方式。

Experimental immunization with anti-rheumatic bacterial extract OM-89 induces T cell responses to heat shock protein (hsp)60 and hsp70; modulation of peripheral immunological tolerance as its possible mode of action in the treatment of rheumatoid arthritis (RA).

作者信息

Bloemendal A, Van der Zee R, Rutten V P, van Kooten P J, Farine J C, van Eden W

机构信息

Institute of Infectious Diseases and Immunology, Utrecht University, The Netherlands.

出版信息

Clin Exp Immunol. 1997 Oct;110(1):72-8. doi: 10.1046/j.1365-2249.1997.4841378.x.

DOI:10.1046/j.1365-2249.1997.4841378.x
PMID:9353151
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1904786/
Abstract

OM-89 is a bacterial (Escherichia coli) extract used for oral administration in the treatment of RA. Given the evidence that immunity to bacterial heat shock antigens plays a critical role in the immunomodulation of arthritis and possibly inflammation in general, the purpose of the present studies was to evaluate the presence and immunogenicity of hsp in OM-89. Furthermore, we studied the effects of OM-89 in an experimental arthritis, where hsp are known to have a critical significance in disease development. In rats immunization with OM-89 was found to lead to proliferative T cell responses to hsp60 and hsp70 of both E. coli and mycobacterial origin. Conversely, immunization with hsp antigens was also found to induce T cell reactivity specific for OM-89. Based on this and the antigen specificity analysis of specific T cell lines, hsp70(DnaK) turned out to be one of the major immunogenic constituents of OM-89. Parenteral immunization with OM-89 was found to reduce resistance to adjuvant arthritis (AA), whereas oral administration was found to protect against AA. Given the arthritis-inhibitory effect of oral OM-89 in AA, it is possible that peripheral tolerance is induced at the level of regulatory T cells with specificity for hsp. This may also constitute a mode of action for OM-89 as an arthritis-suppressive oral drug.

摘要

OM-89是一种用于口服治疗类风湿性关节炎(RA)的细菌(大肠杆菌)提取物。鉴于有证据表明对细菌热休克抗原的免疫在关节炎的免疫调节以及可能在一般炎症中起关键作用,本研究的目的是评估OM-89中热休克蛋白(hsp)的存在情况及其免疫原性。此外,我们研究了OM-89在实验性关节炎中的作用,已知hsp在该疾病发展中具有关键意义。在大鼠中,发现用OM-89免疫会导致对大肠杆菌和分枝杆菌来源的hsp60和hsp70产生增殖性T细胞反应。相反,用hsp抗原免疫也被发现会诱导对OM-89具有特异性的T细胞反应性。基于此以及对特定T细胞系的抗原特异性分析,hsp70(DnaK)被证明是OM-89的主要免疫原性成分之一。发现用OM-89进行肠胃外免疫会降低对佐剂性关节炎(AA)的抵抗力,而口服则被发现可预防AA。鉴于口服OM-89对AA具有关节炎抑制作用,有可能在对hsp具有特异性的调节性T细胞水平上诱导外周耐受。这也可能构成OM-89作为一种抑制关节炎的口服药物的作用方式。